hematological-systemProgrès majeur en Chine dans le traitement de la bêta-thalassémie sévère grâce à l’édition génomique CRISPR
CRISPR gene editing treated children with β0/β0 severe thalassemia have been free from blood transfusion dependence for 3 years, according to the research team, this is also the world's first reported successful clinical result of CRISPR gene editing for the treatment of children with severe thalassemia β0/β0 type.
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